Canonical Allele Identifier: CA379915973
Community Standard Title: NM_004211.5(SLC6A5):c.2122T>C (p.Tyr708His)
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20652340T>C , CM000673.2:g.20652340T>C GRCh38
NC_000011.9:g.20673886T>C , CM000673.1:g.20673886T>C GRCh37
NC_000011.8:g.20630462T>C NCBI36
NG_013086.1:g.57941T>C
NG_013086.2:g.57941T>C

Transcript Alleles

HGVS Amino-acid Change
NM_004211.5:c.2122T>C MANE Select NP_004202.4:p.Tyr708His
ENST00000525748.6:c.2122T>C MANE Select ENSP00000434364.2:p.Tyr708His
NM_001318369.1:c.1420T>C NP_001305298.1:p.Tyr474His
NM_001318369.2:c.1420T>C NP_001305298.1:p.Tyr474His
NM_004211.3:c.2122T>C NP_004202.2:p.Tyr708His
NM_004211.4:c.2122T>C NP_004202.3:p.Tyr708His
ENST00000298923.11:c.*1419T>C ENSP00000298923.7:n.*1419T>C
ENST00000525748.5:c.2122T>C ENSP00000434364.1:p.Tyr708His
ENST00000528440.1:n.653T>C
XM_005253225.1:c.1420T>C XP_005253282.1:p.Tyr474His
XM_011520473.1:c.2122T>C XP_011518775.1:p.Tyr708His
XM_017018544.2:c.1246T>C XP_016874033.1:p.Tyr416His
XM_017018545.2:c.1081T>C XP_016874034.1:p.Tyr361His